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Healthy Adult Male and Female VolunteersFREQNCT07760597

Effects of Exercise Frequency on Muscle Size and Strength in Healthy, Untrained Young Adults

A study testing 10 sessions per week of resistance training and Two sessions per week of resistance training in people with Healthy Adult Male and Female Volunteers, run by Cameron Mitchell at 1 site in Canada.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Resistance training (RT) is important for building and maintaining healthy muscles. An exercise frequency called "exercise snacks" involves short bursts of exercise throughout the day (~5-15 minutes), but no studies have examined a gym-based RT exercise snack program. Read more about this study

Who is it for?
Ages 19 to 39 yearsHealthy volunteers can take part
Conditions the study is for
Healthy Adult Male and Female Volunteers
What is being tested?
10 sessions per week of resistance training and Two sessions per week of resistance training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 siteCanada
Study dates
12 Aug 2026to Jun 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 19 to 39 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Can fluently read and write in English
  • Lives, works, and/or studies at or near the Gateway Health Building (where all study visits will occur)
  • Willing and able to commit to 2 or 10 in-person training sessions per week for 10 continuous weeks, as well as one week of testing before the training period and one week of testing after the training period
  • Has continuous access to smartphone or other device that they can use to access the Technogym app
  • Answers "No" to all questions on the Canadian Society for Exercise Physiology - Get Active Questonnaire (CSEP-GAQ) or has their doctor's approval to participate

Who cannot join

  • Any major uncontrolled cardiovascular, muscular, metabolic, and/or neurological disorders
  • Lung disease, kidney disease, or liver disease
  • Current diagnosis of type 1 diabetes, type 2 diabetes, or cancer
  • Medical conditions that limit their ability to undertake strenuous physical activity
  • Regular use of any medications that may affect muscle physiology or body composition (i.e. benzodiazepines, hormone replacement therapy, ADHD medication, Metformin, Ozempic)
  • Participated in consistent resistance exercise training more than twice per month in the previous 12 months
Show all 13Show fewer
  • Participated in consistent moderate or vigorous aerobic training more than twice per week in the previous 12 months, or planning to start consistent training in the next few months
  • Significant gain or loss of body mass in the past 6 months (greater than 2 kg)
  • Current smoker (including but not limited to cigarettes, e-cigarettes, or vaping)
  • Body Mass Index of less than 18 kg/m2 or over 30 kg/m2
  • Pregnancy or breastfeeding
  • Currently taking blood thinners
  • Allergic to Tegaderm medical tape (used with the activity trackers)

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Cameron Mitchell, PhD contact

604-827-2072

cameron.mitchell@ubc.ca

Canada1 site, 1 recruiting
  • University of British Columbia | Gateway Health Building

    Vancouver, British Columbia, V6T 1Z1

    Cameron Mitchell, PhD, 604-827-2072, cameron.mitchell@ubc.ca

    hdennis@student.ubc.ca

    Recruiting

Other trials in Canada

About this study

Resistance training (RT) is important for building and maintaining healthy muscles. An exercise frequency called "exercise snacks" involves short bursts of exercise throughout the day (~5-15 minutes), but no studies have examined a gym-based RT exercise snack program. The invetigators will randomize 40 participants into one of two groups for 10 weeks: the control group will complete two full-body workouts per week (standard-frequency) and the experimental group will complete 10 mini-workouts per week (high-frequency). Muscle hypertrophy (size) and strength will be measured before and after the exercise program to determine if the participants had the same or different results.

Being tested
10 sessions per week of resistance training, Two sessions per week of resistance training
Keywords
Exerise Snacks, Exercise Frequency, Resistance Training, Muscle Strength, Skeletal Muscle Enlargement, Exercise
Medical subject headings
Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • 10 sessions per week of resistance trainingBehavioural

    Full-body resistance training consisting of 10 sets per week for all major muscle groups with progressive overload in a gym-based setting. Training at an exercise frequency of 10 brief sessions per week (around 8-12 minutes per session).

  • Two sessions per week of resistance trainingBehavioural

    Full-body resistance training consisting of 10 sets per week for all major muscle groups with progressive overload in a gym-based setting. Training at an exercise frequency of two sessions per week (around 45-60 minutes per session).

Study groups in NCT07760597
Study groupRoleWhat they receive
Standard-frequency resistance trainingActive comparatorNot described
Receives: Behavioral: Two sessions per week of resistance training
High-frequency resistance trainingExperimentalNot described
Receives: Behavioral: 10 sessions per week of resistance training

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Total Body Skeletal Muscle Mass Measured using the D3-Creatine Dilution Method

    Measured: From enrolment (Week 1) to the end of the exercise training phase (Week 12)

Secondary outcomes (4)
  1. Change in Total Body Muscle Size Measured as Cross-sectional Area using Muscle Ultrasound Imaging

    Muscle ultrasound imaging will be conducted on one randomly selected side of the body (left or right) for each participant. Scans will be analyzed to determine the cross-sectional area of the following seven muscles: rectus femoris, vastus lateralis, biceps brachii, pectoralis major, latissimus dorsi, triceps brachii, and hamstring group (semitendinosus, semimembranosus, and long head of biceps femoris).

    Measured: From enrolment (Week 1) to the end of the exercise training phase (Week 12)

  2. Change in Muscle Strength Measured as the One-Repetition Maximum of Back Squat and Bench Press

    One-repetition maximums will be measured using a Quantum Synchro Smith Machine.

    Measured: From enrolment (Week 1) to the end of the exercise training phase (Week 12)

  3. Change in Skeletal Muscle Power Measured at Various Relative Loads for Back Squat and Bench Press

    At enrolment (Week 1), power will be measured using a Quantum Synchro Smith Machine at 40%, 50%, 60%, 70%, and 80% of the participant's initial one-repetition maximum (1RM) for back squat and bench press. At the end of the exercise training phase (Week 12), if a participant's 1RM has increased by less than 25%, power will be measured at the same relative loads. If a participant's 1RM has increased by 25-49%, power will be measured at 50%, 60%, 70%, 80%, and 90% of the participant's initial 1RM (in this case, 90% of the participant's initial 1RM would not exceed 80% of the participant's post-training 1RM). If a participant's 1RM has increased by 50% or greater, power will be measured at 60%, 70%, 80%, 90%, and 100% of the participant's initial 1RM (in this case, 100% of the participant's initial 1RM would not exceed 80% of the participant's post-training 1RM).

    Measured: From enrolment (Week 1) to the end of the exercise training phase (Week 12)

  4. Participant Satisfaction with the Exercise Program

    Participant satisfaction with the exercise program will be measured using a modified Intrinsic Motivation Inventory (subscales of "Interest/Enjoyment", "Percieved Competence", "Effort/Importance", and "Value/Usefullness").

    Measured: At the end of the exercise training phase (Week 12)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Aug 2026
  2. Study start12 Aug 2026
  3. Primary completionJun 2027 (estimated)
  4. Study completionJun 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Parallel groups
Model description
At the beginning of the study, participants are assigned to one of two groups for the duration of the study.
Masking
None (open label)
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07760597
Sponsor's protocol ID
H26-01331
Acronym
FREQ
Status last verified
Aug 2026
First submitted
7 Aug 2026
Last updated
13 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: The dataset will contain potentially identifying information (age, height, and weight) of people in a relatively small geographic area, so individual participant data will not be shared with other researchers.

Questions about this trial

What is this clinical trial studying?

A study testing 10 sessions per week of resistance training and Two sessions per week of resistance training in people with Healthy Adult Male and Female Volunteers, run by Cameron Mitchell at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 13 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Cameron Mitchell, PhD (604-827-2072, cameron.mitchell@ubc.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Total Body Skeletal Muscle Mass Measured using the D3-Creatine Dilution Method (time frame: From enrolment (Week 1) to the end of the exercise training phase (Week 12)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Aug 2026.

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